Align Putative bacterial solute-binding protein 1 family (characterized, see rationale)
to candidate WP_069331924.1 C8J29_RS05990 carbohydrate ABC transporter substrate-binding protein
Query= uniprot:A8LLL6 (452 letters) >NCBI__GCF_003046325.1:WP_069331924.1 Length = 450 Score = 593 bits (1530), Expect = e-174 Identities = 282/447 (63%), Positives = 339/447 (75%), Gaps = 4/447 (0%) Query: 7 ASAAALALSAGMAGAGGHLAFTPG-EGEFNWDSYQAFAEATDLSGQDLSIFGPWLAGEAD 65 A AAALAL +G AG L F PG + F+WDS++A + DLSGQ L+I GPWL + Sbjct: 7 AIAAALALVSGPL-AGQELKFPPGADARFHWDSFEAL-KGQDLSGQRLTILGPWLGPDKA 64 Query: 66 AFSNLVAFFNEATGANATYVGSDSLEQQIVIDAEAGSAPDLTVFPQPGLATTMAARGFLT 125 F +++A+F ATGA TY GSD+ EQQIVIDA AGS PD+ VFPQPGLA +A++G L Sbjct: 65 LFDSVIAYFEAATGAEVTYNGSDNFEQQIVIDAGAGSPPDIAVFPQPGLARDLASKGQLA 124 Query: 126 PLPDGTDDWLRENYAAGQSWIDLGTYADGSGNDQLYGFFFNVNVKSLVWYIPENFEDFDY 185 PL T DWLRENYAAG+SW+ LGT+ G + LYGFF+ ++VKSLVWY+PENF DF Y Sbjct: 125 PLDPATADWLRENYAAGESWVSLGTFPGRDGTEALYGFFYKIDVKSLVWYVPENFADFGY 184 Query: 186 EVPETMEEFKALMDQMVEDGQTPLCVGLGSGGATGWPATDWVEDLMLRTQPPEVYDAWVS 245 E+P TMEE +AL ++MV DG TP CVGL SGGATGWPATDWVED+MLR PPEVYD W S Sbjct: 185 EIPATMEELRALTERMVADGVTPWCVGLASGGATGWPATDWVEDMMLRINPPEVYDRWTS 244 Query: 246 NEMPFDDPRVVAAIEEYGSFTRNDDYVVGNANDTASVDFRESPLGLFASPPACMMHRQAS 305 NE+PFDDP+VVAAIEE+G F R D+V G N A+ DFR+SP GLF++PP C MH+QAS Sbjct: 245 NEIPFDDPQVVAAIEEFGWFARTPDFVAGGPNAVAATDFRDSPKGLFSAPPQCFMHKQAS 304 Query: 306 FIPAYFPEGTELGEDADFFYFPAFEEKDLGRPVLGAGTLFAITNENPAASAFIEFLKTPF 365 FIP++FPEGT +GEDADFFY PA+ ++DLG+PVLGAGT+F +T + P A AF+EFLKTP Sbjct: 305 FIPSFFPEGTVIGEDADFFYLPAYADRDLGQPVLGAGTVFGLTRDTPVARAFLEFLKTPI 364 Query: 366 AHEIMMAQDGFLTPFKGANPAAYASDTLRGQGEILTNATTFRFDGSDLMPGGVGAGTFWT 425 AHE+ MAQ GFLTPF G N Y TLR GEIL NATTFRFDGSDLMPG VGAG FWT Sbjct: 365 AHEVWMAQTGFLTPFTGVNTDVYGDPTLRKMGEILLNATTFRFDGSDLMPGAVGAGAFWT 424 Query: 426 GMVDYSSGAKSAADVASEIQASWESLK 452 GM+DY G K A V ++IQ +W++ K Sbjct: 425 GMIDY-MGGKGAERVGADIQRTWDTFK 450 Lambda K H 0.317 0.134 0.413 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 864 Number of extensions: 45 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 452 Length of database: 450 Length adjustment: 33 Effective length of query: 419 Effective length of database: 417 Effective search space: 174723 Effective search space used: 174723 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory